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FDA 510(k)

TR-USB TELEPHONIC STETHOSCOPE

K-Number: K081032 · 2008-06-06

ApplicantRnk Products, Inc.
Decision Date2008-06-06
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TR-USB TELEPHONIC STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Rnk Products, Inc.. It received FDA 510(k) clearance on 2008-06-06 under 510(k) number K081032. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TR-USB TELEPHONIC STETHOSCOPE?

TR-USB TELEPHONIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 2008-06-06. The listed applicant is Rnk Products, Inc.. The 510(k) number is K081032.

When did TR-USB TELEPHONIC STETHOSCOPE receive FDA 510(k) clearance?

TR-USB TELEPHONIC STETHOSCOPE received FDA 510(k) clearance on 2008-06-06, under 510(k) number K081032.

Who is the listed applicant for TR-USB TELEPHONIC STETHOSCOPE?

The FDA 510(k) record lists Rnk Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TR-USB TELEPHONIC STETHOSCOPE?

The FDA product code for TR-USB TELEPHONIC STETHOSCOPE is DQD.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Rnk Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K132405PPA/BT-RB STETHOSCOPEK132560PCP-USB STETHOSCOPEK102893PCP/PC STETHOSCOPEK072026RNK ELECTRONIC STETHOSCOPE

Related Devices (Code: DQD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261494Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart Wireless Stethoscope (STEMO720);Smart Wireless Stethoscope (STEMO730)Shanghai Hulu Devices Co., Ltd.K261694CORE 300 Digital StethoscopeEko Health, Inc.K252915AiSteth®Ai Health Highway India Pvt., Ltd.K252089Tyto Stethoscope (G3)Tyto Care , Ltd.K252076Kneevoice Cartilage Evaluation System (750-3600-001)Kneevoice, Inc.K252284eMurmur Heart AICsd Labs

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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